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FDA 510(k)

BD 呼吸道病毒检测板用于 BD MAX™ 系统;BD 呼吸道病毒检测板-SCV2 用于 BD MAX™ 系统

K号: K230956 · 2023-07-31

决定日期2023-07-31
产品代码QOF
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决定实质等同

器械摘要

BD Respiratory Viral Panel for BD MAX™ System; BD Respiratory Viral Panel-SCV2 for BD MAX™ System is the device name listed in this FDA 510(k) record. The listed applicant is Bd Integrated Diagnostic Solutions /. It received FDA 510(k) clearance on 2023-07-31 under 510(k) number K230956. The device is classified under product code QOF. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the BD Respiratory Viral Panel for BD MAX™ System; BD Respiratory Viral Panel-SCV2 for BD MAX™ System?

BD Respiratory Viral Panel for BD MAX™ System; BD Respiratory Viral Panel-SCV2 for BD MAX™ System is a medical device that received FDA 510(k) clearance on 2023-07-31. The listed applicant is Bd Integrated Diagnostic Solutions /. The 510(k) number is K230956.

When did BD Respiratory Viral Panel for BD MAX™ System; BD Respiratory Viral Panel-SCV2 for BD MAX™ System receive FDA 510(k) clearance?

BD Respiratory Viral Panel for BD MAX™ System; BD Respiratory Viral Panel-SCV2 for BD MAX™ System received FDA 510(k) clearance on 2023-07-31, under 510(k) number K230956.

Who is the listed applicant for BD Respiratory Viral Panel for BD MAX™ System; BD Respiratory Viral Panel-SCV2 for BD MAX™ System?

The FDA 510(k) record lists Bd Integrated Diagnostic Solutions / as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD Respiratory Viral Panel for BD MAX™ System; BD Respiratory Viral Panel-SCV2 for BD MAX™ System?

The FDA product code for BD Respiratory Viral Panel for BD MAX™ System; BD Respiratory Viral Panel-SCV2 for BD MAX™ System is QOF.

相关临床试验

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

相关器械(代码:QOF)

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。

官方来源

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数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。

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